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结缔组织生长因子在骨关节炎中的致病作用。

The pathogenic role of connective tissue growth factor in osteoarthritis.

机构信息

Department of Orthopedics, Second People's Hospital of Jingmen, Jingmen 448000, China.

Department of Gastrointestinal Surgery, Second People's Hospital of Jingmen, Jingmen 448000, China.

出版信息

Biosci Rep. 2019 Jul 18;39(7). doi: 10.1042/BSR20191374. Print 2019 Jul 31.

Abstract

Osteoarthritis (OA) is the most common form of arthritis, and connective tissue growth factor (CTGF) is found to be up-regulated in adjacent areas of cartilage surface damage. CTGF is present in osteophytes of late stage OA. In the present study, we have reviewed association of CTGF in the development and progression of OA and the potential effects of CTGF as a therapeutic agent for the treatment of OA. We have reviewed the recent articles on CTGF and OA in databases like PubMed, google scholar, and SCOPUS and collected the information for the articles. CTGF is usually up-regulated in synovial fluid of OA that stimulates the production of inflammatory cytokines. CTGF also activates nuclear factor-κB, increases the production of chemokines and cytokines, and up-regulates matrix metalloproteinases-3 (MMP-3) that in turn leads to the reduction in proteoglycan contents in joint cartilage. Consequently, cartilage homeostasis is imbalanced that might contribute to the pathogenesis of OA by developing synovial inflammation and cartilage degradation. CTGF might serve as a useful biomarker for the prognosis and treatment of OA, and recent studies have taken attempt to use CTGF as therapeutic target of OA. However, more investigations with clinical trials are necessary to validate the possibility of use of CTGF as a biomarker in OA diagnosis and therapeutic target for OA treatment.

摘要

骨关节炎(OA)是最常见的关节炎形式,已发现连接组织生长因子(CTGF)在软骨表面损伤的相邻区域上调。CTGF 存在于晚期 OA 的骨赘中。在本研究中,我们回顾了 CTGF 在 OA 发展和进展中的关联,以及 CTGF 作为 OA 治疗剂的潜在作用。我们在 PubMed、google scholar 和 SCOPUS 等数据库中查阅了关于 CTGF 和 OA 的最新文章,并收集了这些文章的信息。CTGF 通常在 OA 的滑液中上调,刺激炎症细胞因子的产生。CTGF 还激活核因子-κB,增加趋化因子和细胞因子的产生,并上调基质金属蛋白酶-3(MMP-3),这反过来又导致关节软骨中糖胺聚糖含量减少。因此,软骨动态平衡失衡,通过引发滑膜炎症和软骨降解,可能导致 OA 的发病机制。CTGF 可能作为 OA 预后和治疗的有用生物标志物,最近的研究已经尝试将 CTGF 用作 OA 的治疗靶点。然而,需要更多的临床试验研究来验证 CTGF 作为 OA 诊断生物标志物和 OA 治疗治疗靶点的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8973/6639465/567f702ee3fb/bsr-39-bsr20191374-g1.jpg

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